| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38870535-38870822 | Common:1; Rare:63 | ||||
| chr17:38967369-38967648 | Common:2; Rare:86 | ||||
| chr17:39197520-39197691 | Rare:43 | ||||
| chr17:39197693-39197796 | Common:1; Rare:25 | ||||
| chr17:39199902-39200382 | Common:3; Rare:162 | ||||
| chr17:39200557-39200584 | Common:1; Rare:7 | ||||
| chr17:39401575-39401812 | Common:1; Rare:65 | ||||
| chr17:39451156-39451458 | Common:4; Rare:108 | ||||
| chr17:39461327-39461556 | Common:1; Rare:67 | ||||
| chr17:39461840-39462091 | Common:3; Rare:64 | ||||
| chr17:39636946-39637238 | Common:4; Rare:91 | ||||
| chr17:39687716-39687948 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:39687956-39688224 | Rare:85 | ||||
| chr17:39730205-39730371 | Rare:54 | ||||
| chr17:39730388-39730666 | Common:1; Rare:89 |